FDA•MODERATE
BD PurPrep Sterile Solution
CareFusion is recalling BD PurPrep sterile solution due to a lack of assurance of sterility and potential product contamination.
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FDA•MODERATEWalker Honey: 10 productsWalker Honey recalls Fain's creamed honey spreads over possible stainless steel and plastic particles.
10 products
FDA•MODERATEHorizon Organic Chocolate Lowfat MilkHorizon Organic recalls Chocolate Lowfat Milk 8-oz boxes due to package integrity issues.
FDA•MODERATE...And Kimchi Kimchi...And Kimchi kimchi recalled for undeclared fish allergen.
FDA•MODERATEDELFLEX Peritoneal Dialysis SolutionFresenius recalls DELFLEX dialysis solution due to potential bag leaks compromising sterility.
2 products
FDA•MODERATEDuloxetine Delayed-Release Capsules 30 mgAjanta recalls Duloxetine 30 mg capsules over nitrosamine impurity above FDA limit.
3 products
FDA•MODERATEXZL Jelly SnacksSungal Inc. recalls XZL Jelly Snacks 12.68 oz bags due to undeclared FD&C Yellow #5, #6, and Red #40.
FDA•MODERATEMontebianco Base VeganMontebianco Base Vegan is recalled due to undeclared milk, which exceeds acceptable levels despite the product's warning label.
FDA•MODERATEPhysio-Control LIFEPAK DefibrillatorsPhysio-Control is recalling various LIFEPAK defibrillators serviced without proper performance inspections, potentially delaying therapy.
FDA•MODERATESecond Nature Keto Crunch Smart MixSecond Nature recalls Keto Crunch Smart Mix 10 oz pouches due to undeclared cashews, pistachios, and dried cherries.
FDA•LOWBuspirone Hydrochloride TabletsUnichem is recalling 5 mg buspirone hydrochloride tablets due to subpotency, which may reduce the medication's effectiveness.
FDA•MODERATESpacelabs Ultraview SL Command ModuleSpacelabs is recalling the Ultraview SL Command Module due to a manufacturing issue with the electrical leakage tester.
2 products
FDA•MODERATEProdisc C SK Cervical Disc ImplantCentinel Spine recalls Prodisc C SK cervical disc implants due to labeling mix-up (5mm/6mm).
2 products
FDA•MODERATEBoston Scientific LUX-DX II Arrhythmia DetectorBoston Scientific recalls LUX-DX II Arrhythmia Detector (M302) with LATITUDE DRAGON US Server (6460) over missing PVC Burden and Bradyarrhythmia monitoring.
2 products
FDA•MODERATEERBEFLO CleverCap CO2 Tubing/Cap SetsErbe Medical recalls ERBEFLO CleverCap CO2 tubing/cap sets due to risk of water aspiration and respiratory failure.
3 products- Device RecallFDA•MODERATEda Vinci Surgical System Universal Surgical Manipulator
Intuitive Surgical is recalling the USM arm sub-assembly for da Vinci X and Xi systems due to a risk of internal screw breakage.
2 products 
CPSC•Hepo Adult Portable Bed RailsHepo adult portable bed rails are recalled due to serious entrapment, asphyxiation, fall, and laceration hazards.
CPSC•Acer AES015 Electric ScootersAcer is recalling AES015 electric scooters due to a loose screw that can cause the front tube to collapse, posing a fall hazard.
CPSC•Honda Off-Road MotorcyclesHonda is recalling 2025-2026 off-road motorcycles (CRF250/450 series) due to a handlebar clamp defect that poses a crash hazard.
CPSC•Afrin Original Nasal Spray 6 mLBayer is recalling 6 mL travel size Afrin Original Nasal Spray due to a lack of child-resistant packaging, posing a poisoning risk to children.
CPSC•Malker Bicycle Light SetsMalker is recalling bicycle light sets due to a battery ingestion hazard that can cause serious injury or death.
CPSC•1-K Kerosene Heater Fuel Containers1-K Kerosene Heater Fuel containers are recalled due to missing flame mitigation devices and lack of child-resistant closures.
CPSC•Earthtec Pool Drain CoversEarthtec pool drain covers are recalled due to entrapment and drowning hazards, as they violate federal safety standards.
CPSC•Stephan Baby Boo Bunnie and Friends ToysStephan Baby Boo Bunnie and Friends toys are recalled due to choking and laceration hazards from the toy's plastic cube breaking.
CPSC•Heartwarming Hugs Weighted Plush BearsBuild-A-Bear is recalling Heartwarming Hugs weighted plush bears (model 034464) due to a choking hazard from a detachable zipper slider.
CPSC•UHOMEPRO 5-Drawer DressersUHOMEPRO 5-drawer dressers are recalled due to tip-over and entrapment hazards that violate federal safety standards.
CPSC•DGIVOVO US Electric Pressure WashersDGIVOVO US is recalling model C4012PLUS-1500C electric pressure washers due to shock and electrocution hazards from a missing GFCI.
CPSC•Qumeney Bicycle Light SetsQumeney bicycle light sets (models BL-01 and BL-02) are recalled due to a battery ingestion hazard that can cause serious injury or death.
CPSC•Thermos Stainless King Food Jars and BottlesThermos is recalling Stainless King food jars and bottles because the stoppers can forcefully eject, posing impact and laceration hazards.
CPSC•StrikeLock Hoistway Door Locking DeviceThe StrikeLock hoistway door locking device is recalled due to a risk of serious injury or death from fall hazards.
CPSC•Segmart 4-Drawer DressersSegmart 4-Drawer Dressers are recalled due to tip-over and entrapment hazards, as they fail to meet mandatory safety standards.
FDA•MODERATEMy Mochi Strawberry Non-Dairy Frozen DessertMy Mochi Strawberry Non-Dairy Frozen Dessert recalled due to foreign object in container.
FDA•MODERATECalypso Tropic Tango LemonadeCalypso Tropic Tango Lemonade recalled for undeclared Yellow No. 5.
FDA•MODERATEKLG Kesar MukhwasGanesha Enterprises is recalling KLG Kesar Mukhwas (200 gm) for undeclared food colorings and unapproved dye.
FDA•LOWCVS Lidocaine Wound GelCVS is recalling Lidocaine Wound Gel (NDC 59898-950, 0.5 oz) due to failed pH specifications.
FDA•MODERATEMedline Universal Central/Art Line Insertion KitMedline recalls kits with Webcol Alcohol Prep Pads due to possible non-sterility and contamination risk.
10 products
FDA•MODERATEMedline Neuro SpongesMedline recalls Neuro Sponges (8 sizes) over elevated endotoxin levels.
38 products
FDA•MODERATEAlendronate Sodium Oral Solution 70 mg/75 mLHikma is recalling Alendronate Sodium Oral Solution 70 mg/75 mL (NDC 0054-0282-59) due to out-of-specification assay results.
FDA•MODERATEImmy Myco DDR Trident Neutralization Buffer BImmuno-Mycologics is recalling Myco DDR Trident Neutralization Buffer B due to potential contamination.
FDA•MODERATEATTUNE Revision Hinge FemoralDepuy Synthes recalls ATTUNE Revision Hinge Femoral over packaging adhesion that may compromise sterility.
9 products
FDA•MODERATEepoc BGEM BUN Test CardSiemens is recalling epoc BGEM BUN Test Cards due to inaccurate pH and mTCO2 results that could lead to improper patient treatment.
FDA•MODERATEStraumann n!ce PMMA Full-arch RestorationStraumann recalls n!ce PMMA Full-arch Restoration due to incorrect screw seat interface.
2 products
FDA•MODERATEBD GasPak EZ CO2 Pouch SystemBD recalls GasPak EZ CO2 and Campy pouch systems over low CO2 output.
2 products
FDA•MODERATEPhilips Bridge Prep KitMerit Medical recalls Philips Bridge Prep Kit (REF K12-09098B) over catheter resistance on guidewire.
4 products
FDA•MODERATEi-STAT EG7+ CartridgeAbbott recalls i-STAT EG7+ cartridges (03P76-25) over inaccurate PCO2/pH results.
3 products
FDA•MODERATELeksell Vantage Arc SystemElekta is recalling the Leksell Vantage Arc System due to a risk of coordinate shifting caused by faulty locking mechanisms.
FDA•LOWPALAMIX uno Mixing UnitHeraeus recalls PALAMIX uno mixing units: mixing rod may loosen in units over 17 months old; shelf life reduced to 1.5 years.
2 products
FDA•MODERATEiLet Bionic PancreasBeta Bionics is recalling iLet Bionic Pancreas (software 1.4.2–1.4.3) for Dexcom G7 compatibility issues that may disable glucose correction dosing.
FDA•MODERATEOptase Dry Eye Intense DropsScope Health is recalling Optase Dry Eye Intense Drops (0.33 fl oz, NDC 72972-002-01) due to lack of assurance of sterility.
FDA•MODERATEThea Pharma: Multiple Sterile Lubricant Eye DropsThea Pharma recalls iVIZIA Sterile Lubricant Eye Drops (Povidone 0.5%) over sterility concerns from CGMP deviations.
2 products